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Complex modifier landscape underlying genetic background effects
The phenotypic consequence of a given mutation can be influenced by the genetic background. For example, conditional gene essentiality occurs when the loss of function of a gene causes lethality in one genetic background but not another. Between two individual Saccharomyces cerevisiae strains, S288c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421401/ https://www.ncbi.nlm.nih.gov/pubmed/30804202 http://dx.doi.org/10.1073/pnas.1820915116 |
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author | Hou, Jing Tan, Guihong Fink, Gerald R. Andrews, Brenda J. Boone, Charles |
author_facet | Hou, Jing Tan, Guihong Fink, Gerald R. Andrews, Brenda J. Boone, Charles |
author_sort | Hou, Jing |
collection | PubMed |
description | The phenotypic consequence of a given mutation can be influenced by the genetic background. For example, conditional gene essentiality occurs when the loss of function of a gene causes lethality in one genetic background but not another. Between two individual Saccharomyces cerevisiae strains, S288c and Σ1278b, ∼1% of yeast genes were previously identified as “conditional essential.” Here, in addition to confirming that some conditional essential genes are modified by a nonchromosomal element, we show that most cases involve a complex set of genomic modifiers. From tetrad analysis of S288C/Σ1278b hybrid strains and whole-genome sequencing of viable hybrid spore progeny, we identified complex sets of multiple genomic regions underlying conditional essentiality. For a smaller subset of genes, including CYS3 and CYS4, each of which encodes components of the cysteine biosynthesis pathway, we observed a segregation pattern consistent with a single modifier associated with conditional essentiality. In natural yeast isolates, we found that the CYS3/CYS4 conditional essentiality can be caused by variation in two independent modifiers, MET1 and OPT1, each with roles associated with cellular cysteine physiology. Interestingly, the OPT1 allelic variation appears to have arisen independently from separate lineages, with rare allele frequencies below 0.5%. Thus, while conditional gene essentiality is usually driven by genetic interactions associated with complex modifier architectures, our analysis also highlights the role of functionally related, genetically independent, and rare variants. |
format | Online Article Text |
id | pubmed-6421401 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-64214012019-03-19 Complex modifier landscape underlying genetic background effects Hou, Jing Tan, Guihong Fink, Gerald R. Andrews, Brenda J. Boone, Charles Proc Natl Acad Sci U S A PNAS Plus The phenotypic consequence of a given mutation can be influenced by the genetic background. For example, conditional gene essentiality occurs when the loss of function of a gene causes lethality in one genetic background but not another. Between two individual Saccharomyces cerevisiae strains, S288c and Σ1278b, ∼1% of yeast genes were previously identified as “conditional essential.” Here, in addition to confirming that some conditional essential genes are modified by a nonchromosomal element, we show that most cases involve a complex set of genomic modifiers. From tetrad analysis of S288C/Σ1278b hybrid strains and whole-genome sequencing of viable hybrid spore progeny, we identified complex sets of multiple genomic regions underlying conditional essentiality. For a smaller subset of genes, including CYS3 and CYS4, each of which encodes components of the cysteine biosynthesis pathway, we observed a segregation pattern consistent with a single modifier associated with conditional essentiality. In natural yeast isolates, we found that the CYS3/CYS4 conditional essentiality can be caused by variation in two independent modifiers, MET1 and OPT1, each with roles associated with cellular cysteine physiology. Interestingly, the OPT1 allelic variation appears to have arisen independently from separate lineages, with rare allele frequencies below 0.5%. Thus, while conditional gene essentiality is usually driven by genetic interactions associated with complex modifier architectures, our analysis also highlights the role of functionally related, genetically independent, and rare variants. National Academy of Sciences 2019-03-12 2019-02-25 /pmc/articles/PMC6421401/ /pubmed/30804202 http://dx.doi.org/10.1073/pnas.1820915116 Text en Copyright © 2019 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | PNAS Plus Hou, Jing Tan, Guihong Fink, Gerald R. Andrews, Brenda J. Boone, Charles Complex modifier landscape underlying genetic background effects |
title | Complex modifier landscape underlying genetic background effects |
title_full | Complex modifier landscape underlying genetic background effects |
title_fullStr | Complex modifier landscape underlying genetic background effects |
title_full_unstemmed | Complex modifier landscape underlying genetic background effects |
title_short | Complex modifier landscape underlying genetic background effects |
title_sort | complex modifier landscape underlying genetic background effects |
topic | PNAS Plus |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421401/ https://www.ncbi.nlm.nih.gov/pubmed/30804202 http://dx.doi.org/10.1073/pnas.1820915116 |
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